OBSERVATIONS ON THE MENKES AND BRINDLED MOUSE PHENOTYPES IN CELL HYBRIDS

被引：5

作者：

BROWN, RM ^{[1
]}

CAMAKARIS, J ^{[1
]}

DANKS, DM ^{[1
]}

机构：

[1] UNIV MELBOURNE,DEPT GENET,PARKVILLE,VIC 3052,AUSTRALIA

来源：

SOMATIC CELL AND MOLECULAR GENETICS | 1984年 / 10卷 / 04期

关键词：

D O I：

10.1007/BF01535628

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：321 / 330

页数：10

共 28 条

[11] MENKES KINKY HAIR DISEASE - FURTHER DEFINITION OF DEFECT IN COPPER TRANSPORT [J].

DANKS, DM ;

CARTWRIGHT, E ;

STEVENS, BJ ;

TOWNLEY, RRW .

SCIENCE, 1973, 179 (4078) :1140-1142

[12]

DANKS DM, 1983, ADV HUM GENET, V13, P149

[13] IMPROVED TECHNIQUES FOR INDUCTION OF MAMMALIAN-CELL HYBRIDIZATION BY POLYETHYLENE-GLYCOL [J].

DAVIDSON, RL ;

GERALD, PS .

SOMATIC CELL GENETICS, 1976, 2 (02) :165-176

[14] A SELECTIVE SYSTEM FOR ISOLATION OF HYBRIDS BETWEEN L CELLS AND NORMAL CELLS [J].

DAVIDSON, RL ;

EPHRUSSI, B .

NATURE, 1965, 205 (4977) :1170-&

[15] MENKES DISEASE - BIOCHEMICAL ABNORMALITY IN CULTURED HUMAN FIBROBLASTS [J].

GOKA, TJ ;

STEVENSON, RE ;

HEFFERAN, PM ;

HOWELL, RR .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (02) :604-606

[16]

Green M.C., 1981, GENETIC VARIANTS STR

[17]

HORN N, 1976, LANCET, V1, P1156

[18] PRIMARY DEFECT IN COPPER TRANSPORT UNDERLIES MOTTLED MUTANTS IN MOUSE [J].

HUNT, DM .

NATURE, 1974, 249 (5460) :852-854

[19] ABNORMAL COPPER-METABOLISM AND DEFICIENT LYSYL OXIDASE ACTIVITY IN A HERITABLE CONNECTIVE-TISSUE DISORDER [J].

KUIVANIEMI, H ;

PELTONEN, L ;

PALOTIE, A ;

KAITILA, I ;

KIVIRIKKO, KI .

JOURNAL OF CLINICAL INVESTIGATION, 1982, 69 (03) :730-733

[20]

LABADIE GU, 1983, PEDIATR RES, V17, pA213

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